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Cone and Rod Loss in Stargardt Disease Revealed by Adaptive Optics Scanning Light Ophthalmoscopy

IMPORTANCE: Stargardt disease (STGD1) is characterized by macular atrophy and flecks in the retinal pigment epithelium. The causative ABCA4 gene encodes a protein localizing to photoreceptor outer segments. The pathologic steps by which ABCA4 mutations lead to clinically detectable retinal pigment e...

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Vydáno v:JAMA Ophthalmol
Hlavní autoři: Song, Hongxin, Rossi, Ethan A., Latchney, Lisa, Bessette, Angela, Stone, Edwin, Hunter, Jennifer J., Williams, David R., Chung, Mina
Médium: Artigo
Jazyk:Inglês
Vydáno: 2015
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4600048/
https://ncbi.nlm.nih.gov/pubmed/26247787
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jamaophthalmol.2015.2443
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